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FDA 510(k) Application Details - K183373
Device Classification Name
More FDA Info for this Device
510(K) Number
K183373
Device Name
Bonebridge
Applicant
MED-EL Elektromedizinische Geraete GmbH
Fuerstenweg 77a
Innsbruck 6020 AT
Other 510(k) Applications for this Company
Contact
Stephanie Haselwanter
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
PFO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/06/2018
Decision Date
03/07/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
EN - Ear, Nose, & Throat
Review Advisory Committee
EN - Ear, Nose, & Throat
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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